US3118766A - Photographic products and processes - Google Patents

Photographic products and processes Download PDF

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US3118766A
US3118766A US198763A US19876362A US3118766A US 3118766 A US3118766 A US 3118766A US 198763 A US198763 A US 198763A US 19876362 A US19876362 A US 19876362A US 3118766 A US3118766 A US 3118766A
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gelatin
derivative
anhydride
emulsions
silver halide
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US198763A
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Peter H Roth
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Polaroid Corp
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Polaroid Corp
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Priority to NL121123D priority Critical patent/NL121123C/xx
Priority to BE632933D priority patent/BE632933A/xx
Priority to NL293431D priority patent/NL293431A/xx
Application filed by Polaroid Corp filed Critical Polaroid Corp
Priority to US198763A priority patent/US3118766A/en
Priority to GB15576/63A priority patent/GB1018244A/en
Priority to DEJ23685A priority patent/DE1171264B/en
Priority to FR935949A priority patent/FR1358053A/en
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/047Proteins, e.g. gelatine derivatives; Hydrolysis or extraction products of proteins

Definitions

  • silver halide emulsions are prepared by reacting a water-soluble silver salt, such as silver nitrate, with at least one water-soluble halide such as potassium bromide, sodium bromide, potassium iodide or sodium iodide in an aqueous solution comprising a peptizing agent such, for example, as gelatin.
  • a water-soluble silver salt such as silver nitrate
  • water-soluble halide such as potassium bromide, sodium bromide, potassium iodide or sodium iodide
  • the dispersion of silver halide thus formed also contains water-soluble salts, produced by the double decomposition reaction, and usually excess reagents. It has been generally found desirable to remove such water-soluble salts and reagents.
  • One method employed comprises having present in the silver halide dispersion, at least after its formation, an acid-coagulable derivative of gelatin, and lowering the pH to bring about precipitation.
  • the acid-coagulable derivatives Upon precipitation, the acid-coagulable derivatives carry the silver halide salts with them, leaving the soluble salts in solution, for removal by decantation. When desired, the precipitate may be washed to remove additional salts.
  • the present invention is concerned with improved processes of this nature.
  • One object of the present invention is to provide processes for preparing silver halide emulsions which employ novel acid-coagulable derivatives of gelatin and which produce emulsions having increased speed.
  • the invention accordingly comprises the process involving the several steps and the relation and order of one or more of such steps with respect to each of the others and the product possessing the features, properties and the relation of components which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
  • the trimellitic acid anhydride derivative of gelatin is used as the peptizing agent during the formation of the silver halide salt.
  • the soluble silver salt and the soluble halide salt are added, with vigorous stirring, to an aqueous solution comprising the trimellitic acid anhydride derivative.
  • the pH of the resulting dispersion is lowered by the addition of a suitable acid such, for example, as a mineral acid, until coagulation takes place and the silver halide and gelatin derivative precipitate out.
  • a suitable acid such as a mineral acid
  • the resulting precipitate is then separated from the supernatant ice liquid and, when desired, washed.
  • the resulting precipitate may be redispersed for further compounding by raising the pH through the addition of a suitable base such, for example, as ammonium hydroxide, sodium hydroxide, etc.
  • the silver halide is prepared in the presence of a regular peptizing agent such, for example, as gelatin and the trimellitic acid anhydride derivative is subsequently added.
  • a regular peptizing agent such as gelatin and the trimellitic acid anhydride derivative is subsequently added.
  • the ratio, by weight, of derivative to the instant peptizing agent will be at least 1 to 3, preferably it will be at least 1 to 1 and more preferably at least 2 to 1.
  • a much higher ratio may be employed, e.g., 10 to 1.
  • the derivative precipitates out carrying with it the gelatin and the silver halide.
  • the silver halide emulsions prepared by the processes of this invention may be further compounded with additional gelatin, gelatin derivaties or other protective colloids.
  • the gelatin derivatives of this invention may be prepared by reacting gelatin with the trimellitic acid anhydride in an alkaline medium. Preferably the reaction is carried out at a pH of about 8 to 10 at a temperature of about 20 to 60.
  • the amount of anhydride employed may be varied over a considerable range. Generally use of at least about 5%, by weight, of the anhydride based on the weight of the gelatin will be effective. Especially good results have been obtained by using about 10%, by weight, of the anhydride based on the weight of the gelatin.
  • Example 1 A 10% aqueous gelatin solution, having a pH of about 8.5, was prepared and heated to about 50 C. Over a 30 minute period an amount of trimellitic anhydride equal to about 10%, by weight, of the gelatin was stirred in while maintaining the temperature at about 50 C. and the pH at about 8.5. After the trimellitic anhydride was completely added the reaction was continued for about 15 minutes while maintaining the temperature-and pH at the initial levels. The solution was then adjusted to a final pH of about 6.2.
  • Example 2 A 20 ml. portion of a silver nitrate solution comprising 10 g. of silver nitrate and ml. of water was added with rapid stirring to a solution comprising 220 ml. of water, 18.2 g. ammonium bromide, 3 ml. of a 10% potassium iodide solution, 1.5 ml. of concentrated ammonia Water and 10 g. of a gelatin-trimellitic anhydride derivative as prepared in Example 1. The balance of the silver nitrate solution was then added over a 12 minute period. After a pause of 5 minutes, half of a second silver nitrate solution comprising 120 ml. of water and 20 g. silver nitrate was then added.
  • the emulsions of the present invention may be chemically sensitized by any of the accepted procedures.
  • the emulsions may be digested with naturally active gelatin, or sulfur compounds can be added such as those described in U.S. Patents Nos. 1,574,944, 1,623,499, and 2,410,689.
  • the emulsions may also be treated with salts of the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum, all of which belong to group VIII of the periodic table of elements and have an atomic weight greater than 100.
  • the salts may be used for sensitizing in amounts below that which produce any substantial fog inhibition, as described in U.S. Patent No. 2,448,060, and as antifoggants in higher amounts, as described in US. Patents Nos. 2,566,245 and 2,566,263.
  • the emulsions may also be chemically sensitized with gold salts as described in US. Patent No. 2,399,083 or stabilized with gold salts as described in U.S. Patents Nos. 2,597,856 and 2,597,915.
  • the emulsions may further be chemically sensitized with reducing agents such as stannous chloride as described in US. Patent No. 2,487,850; amines such as diethylenetriamine as described in US. Patent No. 2,518,-
  • reducing agents such as stannous chloride as described in US. Patent No. 2,487,850; amines such as diethylenetriamine as described in US. Patent No. 2,518,-
  • polyamides such as spermine as described in US.
  • Patent No. 2,521,925 or bis-(fi-aminoethyl)-sulfide and its water-soluble salts as described in US. Patent No. 2,521,926.
  • the emulsions may also be stabilized with the mercury compounds of US. Patents Nos. 2,728,663, 2,728,664, and 2,728,665.
  • the emulsions may also be optically sensitized with cyanine and merocyanine dyes as described in US. Patents Nos. 1,846,301, 1,846,302, 1,942,854, 1,990,507, 2,112,140, 2,165,338, 2,493,747, 2,493,748, 2,503,776, 2,519,001, 2,666,761, 2,734,900, 2,739,149 and 2,739,964.
  • the emulsions may also contain speed-increasing compounds of the quaternary ammonium type as described in US. Patents Nos. 2,271,623, 2,288,226 and 2,334,864, and of the polyethylene glycol type as described in US. Patent No. 2,708,162.
  • Suitable reagents such for example as antifoggants, restrainers, accelerators, preservatives, coating aids, and/or stabilizers may be included in the composition of the emulsions.
  • a method of preparing silver halide emulsions which comprises, in combination, the steps of mixing together a water-soluble silver salt and at least one water soluble halide salt in an aqueous solution comprising a peptizing agent to form therein a dispersion of silver halide, said dispersion having therein, at least after formation, an acid-coagulable derivative of gelatin with trimellitic acid anhydride; the ratio, by weight, of said derivative to said peptizing agent being at least 1 to 3; subsequently lowering the pH to bring about precipitation and separating the precipitated silver halide emulsion from the supernatant liquid.
  • a process as defined in claim 1 wherein said derivative is prepared by reacting gelatin with at least 5% by Weight, based on said gelatin, of trimellitic acid anhydride.
  • a process as defined in claim 1 wherein said derivative is prepared by reacting gelatin with about 10% by weight, based on said gelatin, of trimellitic acid anhydride.
  • a method of preparing silver halide emulsions which comprises, in combination, the steps of mixing together a water-soluble silver salt and at least one water-soluble halide salt in an aqueous solution comprising a peptizing agent to form therein a dispersion of silver halide, said dispersion having therein, at least after formation, an acidcoagulable derivative of gelatin with trimellitic acid anhydride, said derivative of gelatin with trimellitic acid anhydride being prepared by reacting gelatin with at least 5% by weight, based on said gelatin, of trimellitic anhydride; the ratio, by weight, of said derivative to said peptizing agent being at least about 1 to 1, by weight; subsequently lowering the pH to between about 4.5 to about 2.0 to bring about precipitation and separating the precipitated silver halide emulsion from the supernatant liquid.
  • a process as defined in claim 9 wherein said derivative is prepared by reacting gelatin with about 10%, by weight, based on said gelatin, of trimellitic acid anhydride.
  • a photographic product comprising a colloid carrier and a light-sensitive silver halide, said carrier comprising a derivative of gelatin with trimellitic anhydride.
  • a product as defined in claim 13 wherein said de rivative is prepared by reacting gelatin with at least 5%, by weight, based on said gelatin, of trimellitic acid anhydride.

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  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)

Description

United States Patent 3,118,766 PHOTOGRAPHHC PRODUCTS AND PROCESSES Peter H. Roth, Watertown, Mass., assignor to Polaroid Corporation, Cambridge, Mass., a corporation of Delaware No Drawing. Filed May 31, 1962, Ser. No. 198,763 Claims. (Cl. 96114) The present invention is concerned with the preparation of photographic silver halide emulsions and more particularly with. the preparation of emulsions having improved photographic properties.
Generally, silver halide emulsions are prepared by reacting a water-soluble silver salt, such as silver nitrate, with at least one water-soluble halide such as potassium bromide, sodium bromide, potassium iodide or sodium iodide in an aqueous solution comprising a peptizing agent such, for example, as gelatin. The dispersion of silver halide thus formed also contains water-soluble salts, produced by the double decomposition reaction, and usually excess reagents. It has been generally found desirable to remove such water-soluble salts and reagents. One method employed comprises having present in the silver halide dispersion, at least after its formation, an acid-coagulable derivative of gelatin, and lowering the pH to bring about precipitation. Upon precipitation, the acid-coagulable derivatives carry the silver halide salts with them, leaving the soluble salts in solution, for removal by decantation. When desired, the precipitate may be washed to remove additional salts. As examples of such processes mention may be made of those disclosed in US. Patents Nos. 2,614,928, 2,614,929, and 2,728,662 wherein aromatic sulfonyl chloride, carboxylic acid chloride and carboxylic acid anhdydride derivatives of gelatin are employed as the acid-coagulable materials. The present invention is concerned with improved processes of this nature.
One object of the present invention is to provide processes for preparing silver halide emulsions which employ novel acid-coagulable derivatives of gelatin and which produce emulsions having increased speed.
Other objects of the invention will in part be obvious and will in part appear hereinafter.
The invention accordingly comprises the process involving the several steps and the relation and order of one or more of such steps with respect to each of the others and the product possessing the features, properties and the relation of components which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
For a fuller understanding of the nature and objects of the invention, reference should be had to the following etailed description.
It has been found in the present invention that when gelatin derivatives of trimellitic acid anhydride, i.e., the 1,2 anhydride of 1,2,4-benzene tricarboxylic acid, are used as the acid-coagulable material in the precipitation step, the resulting emulsions have increased speed and are more responsive to chemical sensitizers.
in a preferred mode of carrying out the present invention, the trimellitic acid anhydride derivative of gelatin is used as the peptizing agent during the formation of the silver halide salt. In such an embodiment, the soluble silver salt and the soluble halide salt are added, with vigorous stirring, to an aqueous solution comprising the trimellitic acid anhydride derivative. Subsequent to the silver halide formation, the pH of the resulting dispersion is lowered by the addition of a suitable acid such, for example, as a mineral acid, until coagulation takes place and the silver halide and gelatin derivative precipitate out. Usually, lowering the pH to a range of from about 4.5 to about 2 will bring about such precipitation. The resulting precipitate is then separated from the supernatant ice liquid and, when desired, washed. The resulting precipitate may be redispersed for further compounding by raising the pH through the addition of a suitable base such, for example, as ammonium hydroxide, sodium hydroxide, etc.
In another mode of carrying out the processes of the present invention, the silver halide is prepared in the presence of a regular peptizing agent such, for example, as gelatin and the trimellitic acid anhydride derivative is subsequently added. Generally the ratio, by weight, of derivative to the instant peptizing agent will be at least 1 to 3, preferably it will be at least 1 to 1 and more preferably at least 2 to 1. When desired, a much higher ratio may be employed, e.g., 10 to 1. Upon lowering the pH, the derivative precipitates out carrying with it the gelatin and the silver halide.
The silver halide emulsions prepared by the processes of this invention may be further compounded with additional gelatin, gelatin derivaties or other protective colloids.
The gelatin derivatives of this invention may be prepared by reacting gelatin with the trimellitic acid anhydride in an alkaline medium. Preferably the reaction is carried out at a pH of about 8 to 10 at a temperature of about 20 to 60. The amount of anhydride employed may be varied over a considerable range. Generally use of at least about 5%, by weight, of the anhydride based on the weight of the gelatin will be effective. Especially good results have been obtained by using about 10%, by weight, of the anhydride based on the weight of the gelatin.
The following non-limiting example illustrates the prep aration of gelatin derivatives within the scope of this invention.
Example 1 A 10% aqueous gelatin solution, having a pH of about 8.5, was prepared and heated to about 50 C. Over a 30 minute period an amount of trimellitic anhydride equal to about 10%, by weight, of the gelatin was stirred in while maintaining the temperature at about 50 C. and the pH at about 8.5. After the trimellitic anhydride was completely added the reaction was continued for about 15 minutes while maintaining the temperature-and pH at the initial levels. The solution was then adjusted to a final pH of about 6.2.
The following non-limiting example illustrates the preparation of a silver halide emulsion through the processes of the present invention.
Example 2 A 20 ml. portion of a silver nitrate solution comprising 10 g. of silver nitrate and ml. of water was added with rapid stirring to a solution comprising 220 ml. of water, 18.2 g. ammonium bromide, 3 ml. of a 10% potassium iodide solution, 1.5 ml. of concentrated ammonia Water and 10 g. of a gelatin-trimellitic anhydride derivative as prepared in Example 1. The balance of the silver nitrate solution was then added over a 12 minute period. After a pause of 5 minutes, half of a second silver nitrate solution comprising 120 ml. of water and 20 g. silver nitrate was then added. After a further pause of about 10 minutes, the balance of the second silver nitrate solution was added. The resulting emulsion was precipitated by reducing the pH to 3 with sulfuric acid. The precipitate was then washed until the supernatant water had a resistivity of 4000 ohm-cm. Thirty grams of an inert after-ripening gelatin was then added and the volume was adjusted with water to 600 ml. The gel was dissolved by heating to 35 C. and adjusting the pH to 6.0 and the pAg to 8.75. At this point, 0.5 ml. of a 0.1% sodium thiosulfate solution and 0.5 ml. of a 0.1% gold Gelatin Derivative Used for Speed Fog Gamma D Max.
Making- Irimellitic anhydride 260 0.10 0. 40 1. 74 Succinic anhydride 114 0.09 0.30 1. 38 Ihtlialic anhydride 200 0.16 O. 36 1.50 Benzene sulphonyl chloride 158 0.10 0. 46 1. 46 Maleie anhydride 158 0.10 0. 46 1. 80
As can be noted a substantial increase in speed was obtained using the trimellitic anhydride derivative.
The emulsions of the present invention may be chemically sensitized by any of the accepted procedures. For example, the emulsions may be digested with naturally active gelatin, or sulfur compounds can be added such as those described in U.S. Patents Nos. 1,574,944, 1,623,499, and 2,410,689.
The emulsions may also be treated with salts of the noble metals such as ruthenium, rhodium, palladium, iridium, and platinum, all of which belong to group VIII of the periodic table of elements and have an atomic weight greater than 100. The salts may be used for sensitizing in amounts below that which produce any substantial fog inhibition, as described in U.S. Patent No. 2,448,060, and as antifoggants in higher amounts, as described in US. Patents Nos. 2,566,245 and 2,566,263.
The emulsions may also be chemically sensitized with gold salts as described in US. Patent No. 2,399,083 or stabilized with gold salts as described in U.S. Patents Nos. 2,597,856 and 2,597,915.
The emulsions may further be chemically sensitized with reducing agents such as stannous chloride as described in US. Patent No. 2,487,850; amines such as diethylenetriamine as described in US. Patent No. 2,518,-
698; polyamides such as spermine as described in US.
Patent No. 2,521,925; or bis-(fi-aminoethyl)-sulfide and its water-soluble salts as described in US. Patent No. 2,521,926.
The emulsions may also be stabilized with the mercury compounds of US. Patents Nos. 2,728,663, 2,728,664, and 2,728,665.
The emulsions may also be optically sensitized with cyanine and merocyanine dyes as described in US. Patents Nos. 1,846,301, 1,846,302, 1,942,854, 1,990,507, 2,112,140, 2,165,338, 2,493,747, 2,493,748, 2,503,776, 2,519,001, 2,666,761, 2,734,900, 2,739,149 and 2,739,964.
The emulsions may also contain speed-increasing compounds of the quaternary ammonium type as described in US. Patents Nos. 2,271,623, 2,288,226 and 2,334,864, and of the polyethylene glycol type as described in US. Patent No. 2,708,162.
Where desired, other suitable reagents such for example as antifoggants, restrainers, accelerators, preservatives, coating aids, and/or stabilizers may be included in the composition of the emulsions.
Since certain changes may be made in the above process and product Without departing from the scope of the invention herein involved, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
What is claimed is:
l. A method of preparing silver halide emulsions which comprises, in combination, the steps of mixing together a water-soluble silver salt and at least one water soluble halide salt in an aqueous solution comprising a peptizing agent to form therein a dispersion of silver halide, said dispersion having therein, at least after formation, an acid-coagulable derivative of gelatin with trimellitic acid anhydride; the ratio, by weight, of said derivative to said peptizing agent being at least 1 to 3; subsequently lowering the pH to bring about precipitation and separating the precipitated silver halide emulsion from the supernatant liquid.
2. A process as defined in claim 1 wherein the ratio of said derivative to said peptizing agent is at least 1 to 1 by weight.
3. A process as defined in claim 1 wherein the ratio of said derivative to said peptizing agent is at least 2 to l by weight.
4. A process as defined in claim 1 wherein said derivative is added subsequent to the formation of said dispersicn.
5. A process as defined in claim 1 wherein said derivative is prepared by reacting gelatin with at least 5% by Weight, based on said gelatin, of trimellitic acid anhydride.
6. A process as defined in claim 1 wherein said derivative is prepared by reacting gelatin with about 10% by weight, based on said gelatin, of trimellitic acid anhydride.
7. A process as defined in claim 1 wherein said pH is lowered to between about 4.5 to about 2.0.
8. A process as defined in claim 1 wherein said derivative of gelatin with trimellitic acid anhydride is initially present as the peptizing agent.
9. A method of preparing silver halide emulsions which comprises, in combination, the steps of mixing together a water-soluble silver salt and at least one water-soluble halide salt in an aqueous solution comprising a peptizing agent to form therein a dispersion of silver halide, said dispersion having therein, at least after formation, an acidcoagulable derivative of gelatin with trimellitic acid anhydride, said derivative of gelatin with trimellitic acid anhydride being prepared by reacting gelatin with at least 5% by weight, based on said gelatin, of trimellitic anhydride; the ratio, by weight, of said derivative to said peptizing agent being at least about 1 to 1, by weight; subsequently lowering the pH to between about 4.5 to about 2.0 to bring about precipitation and separating the precipitated silver halide emulsion from the supernatant liquid.
10. A process as defined in claim 9 wherein said derivative is added subsequent to the formation of said dispersron.
11. A process as defined in claim 9 wherein said derivative is prepared by reacting gelatin with about 10%, by weight, based on said gelatin, of trimellitic acid anhydride.
12. A process as defined in claim 9 wherein said derivative of gelatin with trimellitic acid anhydride is initially present as the peptizing agent.
13. A photographic product comprising a colloid carrier and a light-sensitive silver halide, said carrier comprising a derivative of gelatin with trimellitic anhydride.
14. A product as defined in claim 13 wherein said de rivative is prepared by reacting gelatin with at least 5%, by weight, based on said gelatin, of trimellitic acid anhydride.
15. A product as defined in claim 14 wherein 10% of said trimellitic anhydride is used.
References Cited in the file of this patent UNITED STATES PATENTS 2,403,428 Mueller et al July 2, 1946 2,614,929 Yutzy et al Oct. 21, 1952 2,888,465 Hodes May 26, 1959 OTHER REFERENCES Tajima et 211.: Chemical Abstracts, vol. 53, p. 3958 (1959).

Claims (1)

1. THE METHOD OF PREPARING SILVER HALIDE EMULSIONS WHICH COMPRISES, IN COMBINATION, THE STEPS OF MIXING TOGETHER A WATER-SOLUBLE SILVER SALT AND AT LEAST ONE WATERSOLUBLE HALIDE SALT IN AN AQUEOUS SOLUTION COMPRISING A PEPTIZING AGENT TO FORM THEREIN A DISPERSION OF SIVLER HALIDE, SAID DISPERSION HAVING THEREIN, AT LEAST AFTER FORMATION, AN ACID-COAGULABLE DERIVATIVE OF GELATIN WITH TRIMELLITIC ACID ANHYDRIDE; THE RATIO, BY WEIGHT, OF SAID DERIVATIVE TO SAID PEPTIZING AGENT BEING AT LEAST 1 TO 3; SUBSEQUENTLY LOWERING THE PH TO BRING ABOUT PRECIPITATION AND SEPARARTING THE PRECIPITATED SILVER HADLIDE EMULSION FROM THE SUPERNATANT LIQUID.
US198763A 1962-05-31 1962-05-31 Photographic products and processes Expired - Lifetime US3118766A (en)

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Application Number Priority Date Filing Date Title
NL121123D NL121123C (en) 1962-05-31
BE632933D BE632933A (en) 1962-05-31
NL293431D NL293431A (en) 1962-05-31
US198763A US3118766A (en) 1962-05-31 1962-05-31 Photographic products and processes
GB15576/63A GB1018244A (en) 1962-05-31 1963-04-19 Photographic emulsions and gelatin derivative for use therein
DEJ23685A DE1171264B (en) 1962-05-31 1963-05-10 Process for the preparation of photographic silver halide emulsions by the flocculation process
FR935949A FR1358053A (en) 1962-05-31 1963-05-24 Photographic products and processes

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3282698A (en) * 1962-01-15 1966-11-01 Gevaert Photo Prod Nv Photographic stripping films
US4363864A (en) * 1978-05-10 1982-12-14 Minnesota Mining And Manufacturing Company Colloid relief images by oxidized developer transfer
US4444926A (en) * 1980-11-10 1984-04-24 Fuji Photo Film Co., Ltd. Method of hardening gelatin and photographic materials produced thereby
EP0200206A2 (en) 1985-04-30 1986-11-05 Konica Corporation Silver halide photographic light-sensitive material
EP0201027A2 (en) 1985-04-30 1986-11-12 Konica Corporation Silver halide photographic light-sensitive material
EP0202784A2 (en) 1985-04-23 1986-11-26 Konica Corporation Silver halide photographic light-sensitive material
EP0209118A2 (en) 1985-07-17 1987-01-21 Konica Corporation Silver halide photographic material
US5989800A (en) * 1996-11-19 1999-11-23 Fuji Photo Film Co., Ltd Process for producing tabular silver halide grains
EP1364802A2 (en) 2002-05-21 2003-11-26 FERRANIA S.p.A. Receiving sheet for ink-jet printing
WO2005072974A1 (en) 2004-01-16 2005-08-11 Eastman Kodak Company Mordanted inkjet recording element and printing method
WO2012035314A1 (en) 2010-09-17 2012-03-22 Fujifilm Manufacturing Europe Bv Photographic paper
WO2021213762A1 (en) 2020-04-24 2021-10-28 Fujifilm Manufacturing Europe Bv Photographic paper

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US2403428A (en) * 1942-09-30 1946-07-02 Gen Aniline & Film Corp Intensification of the latent image
US2614929A (en) * 1947-08-13 1952-10-21 Eastman Kodak Co Method of preparing photographic emulsions
US2888465A (en) * 1957-05-27 1959-05-26 Standard Oil Co Process for the preparation of trimellitic anhydride

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Publication number Priority date Publication date Assignee Title
BE484326A (en) * 1947-08-13
US2614931A (en) * 1947-08-13 1952-10-21 Eastman Kodak Co Method of preparing cellulose ester-silver-halide photographic emulsions

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Publication number Priority date Publication date Assignee Title
US2403428A (en) * 1942-09-30 1946-07-02 Gen Aniline & Film Corp Intensification of the latent image
US2614929A (en) * 1947-08-13 1952-10-21 Eastman Kodak Co Method of preparing photographic emulsions
US2888465A (en) * 1957-05-27 1959-05-26 Standard Oil Co Process for the preparation of trimellitic anhydride

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3282698A (en) * 1962-01-15 1966-11-01 Gevaert Photo Prod Nv Photographic stripping films
US4363864A (en) * 1978-05-10 1982-12-14 Minnesota Mining And Manufacturing Company Colloid relief images by oxidized developer transfer
US4444926A (en) * 1980-11-10 1984-04-24 Fuji Photo Film Co., Ltd. Method of hardening gelatin and photographic materials produced thereby
EP0202784A2 (en) 1985-04-23 1986-11-26 Konica Corporation Silver halide photographic light-sensitive material
EP0200206A2 (en) 1985-04-30 1986-11-05 Konica Corporation Silver halide photographic light-sensitive material
EP0201027A2 (en) 1985-04-30 1986-11-12 Konica Corporation Silver halide photographic light-sensitive material
EP0209118A2 (en) 1985-07-17 1987-01-21 Konica Corporation Silver halide photographic material
US5989800A (en) * 1996-11-19 1999-11-23 Fuji Photo Film Co., Ltd Process for producing tabular silver halide grains
EP1364802A2 (en) 2002-05-21 2003-11-26 FERRANIA S.p.A. Receiving sheet for ink-jet printing
WO2005072974A1 (en) 2004-01-16 2005-08-11 Eastman Kodak Company Mordanted inkjet recording element and printing method
WO2012035314A1 (en) 2010-09-17 2012-03-22 Fujifilm Manufacturing Europe Bv Photographic paper
WO2021213762A1 (en) 2020-04-24 2021-10-28 Fujifilm Manufacturing Europe Bv Photographic paper

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